1re3
From Proteopedia
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==About this Structure== | ==About this Structure== | ||
| - | 1RE3 is a | + | 1RE3 is a 8 chains structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1RE3 OCA]. |
==Reference== | ==Reference== | ||
| - | + | <ref group="xtra">PMID:14992584</ref><references group="xtra"/> | |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
| - | [[Category: Protein complex]] | ||
[[Category: Betts, L.]] | [[Category: Betts, L.]] | ||
[[Category: Gorkun, O V.]] | [[Category: Gorkun, O V.]] | ||
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[[Category: Variant fibrinogen]] | [[Category: Variant fibrinogen]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 23:41:17 2009'' |
Revision as of 21:41, 16 February 2009
Contents |
Crystal Structure of Fragment D of BbetaD398A Fibrinogen with the Peptide Ligand Gly-His-Arg-Pro-Amide
Template:ABSTRACT PUBMED 14992584
Disease
Known disease associated with this structure: Afibrinogenemia, congenital OMIM:[134820], Amyloidosis, hereditary renal OMIM:[134820], Dysfibrinogenemia, alpha type, causing bleeding diathesis OMIM:[134820], Dysfibrinogenemia, alpha type, causing recurrent thrombosis OMIM:[134820], Afibrinogenemia, congenital OMIM:[134830], Dysfibrinogenemia, beta type OMIM:[134830], Thrombophilia, dysfibrinogenemic OMIM:[134830], Dysfibrinogenemia, gamma type OMIM:[134850], Hypofibrinogenemia, gamma type OMIM:[134850], Thrombophilia, dysfibrinogenemic OMIM:[134850]
About this Structure
1RE3 is a 8 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Kostelansky MS, Bolliger-Stucki B, Betts L, Gorkun OV, Lord ST. B beta Glu397 and B beta Asp398 but not B beta Asp432 are required for "B:b" interactions. Biochemistry. 2004 Mar 9;43(9):2465-74. PMID:14992584 doi:10.1021/bi035996f
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